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- W3178172899 endingPage "1384" @default.
- W3178172899 startingPage "1373" @default.
- W3178172899 abstract "Pulmonary fibrosis is a chronic debilitating condition characterized by progressive deposition of connective tissue, leading to a steady restriction of lung elasticity, a decline in lung function, and a median survival of 4.5 years. The leading causes of pulmonary fibrosis are inhalation of foreign particles (such as silicosis and pneumoconiosis), infections (such as post COVID-19), autoimmune diseases (such as systemic autoimmune diseases of the connective tissue), and idiopathic pulmonary fibrosis. The therapeutics currently available for pulmonary fibrosis only modestly slow the progression of the disease. This review is centered on the interplay of damage-associated molecular pattern (DAMP) molecules, Toll-like receptor 4 (TLR4), and inflammatory cytokines (such as TNF-α, IL-1β, and IL-17) as they contribute to the pathogenesis of pulmonary fibrosis, and the possible avenues to develop effective therapeutics that disrupt this interplay." @default.
- W3178172899 created "2021-07-19" @default.
- W3178172899 creator A5008416216 @default.
- W3178172899 creator A5084966628 @default.
- W3178172899 creator A5090798506 @default.
- W3178172899 date "2021-07-13" @default.
- W3178172899 modified "2023-10-03" @default.
- W3178172899 title "The interplay of DAMPs, TLR4, and proinflammatory cytokines in pulmonary fibrosis" @default.
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